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Released exopolysaccharide (r-EPS) produced from probiotic bacteria reduce biofilm formation of enterohemorrhagic Escherichia coli O157:H7

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dc.contributor.authorKim, Younghoon-
dc.contributor.authorOh, Sejong-
dc.contributor.authorKim, Sae Hun-
dc.date.accessioned2021-09-08T19:54:52Z-
dc.date.available2021-09-08T19:54:52Z-
dc.date.created2021-06-19-
dc.date.issued2009-02-06-
dc.identifier.issn0006-291X-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/120588-
dc.description.abstractHere, we characterized released-exopolysaccharides (r-EPS) from Lactobacillus acidophilus A4 with the goal of identifying natural compounds that represses biofilm formation. In plastic 96-well microplates that contained 1.0 mg/ml of r-EPS, enterohemorrhagic Escherichia coli (EHEC) biofilms were dramatically decreased by 87% and 94% on polystyrene and polyvinyl chloride (PVC) surfaces, respectively. In the presence of r-EPS, neither their growth rate nor their autoinducer-2-like activity was affected on the EHEC O157:H7. Importantly, consistent reduction in biofilm formation was also observed when r-EPS was applied to the continuous-flow chamber models. In addition, we found that adding r-EPS significantly repressed biofilm formation by affecting genes related to curli production (crl, csgA. and csgB) and chemotaxis (cheY) in transcriptome analysis. Furthermore, these r-EPS Could prevent biofilm formation by a wide range of Gram-negative and -positive pathogens. This property may lead to the development of novel food-grade adjuncts for microbial biofilm control. (c) 2008 Elsevier Inc. All rights reserved.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherACADEMIC PRESS INC ELSEVIER SCIENCE-
dc.subjectDIFFERENTIAL GENE-EXPRESSION-
dc.subjectO157-H7-
dc.subjectAUTOAGGREGATION-
dc.subjectINHIBITION-
dc.subjectMOTILITY-
dc.titleReleased exopolysaccharide (r-EPS) produced from probiotic bacteria reduce biofilm formation of enterohemorrhagic Escherichia coli O157:H7-
dc.typeArticle-
dc.contributor.affiliatedAuthorKim, Sae Hun-
dc.identifier.doi10.1016/j.bbrc.2008.12.053-
dc.identifier.scopusid2-s2.0-58249139318-
dc.identifier.wosid000262924300031-
dc.identifier.bibliographicCitationBIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, v.379, no.2, pp.324 - 329-
dc.relation.isPartOfBIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS-
dc.citation.titleBIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS-
dc.citation.volume379-
dc.citation.number2-
dc.citation.startPage324-
dc.citation.endPage329-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaBiophysics-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryBiophysics-
dc.subject.keywordPlusDIFFERENTIAL GENE-EXPRESSION-
dc.subject.keywordPlusO157-H7-
dc.subject.keywordPlusAUTOAGGREGATION-
dc.subject.keywordPlusINHIBITION-
dc.subject.keywordPlusMOTILITY-
dc.subject.keywordAuthorEHEC O157:H7-
dc.subject.keywordAuthorLactobacillus acidophilus-
dc.subject.keywordAuthorBiofilm formation-
dc.subject.keywordAuthorExopolysaccharide-
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